Multiple cranial nerve palsies as the presenting feature of meningeal myelomatosis
نویسندگان
چکیده
منابع مشابه
Tumors Presenting as Multiple Cranial Nerve Palsies
Cranial nerve palsy could be one of the presenting features of underlying benign or malignant tumors of the head and neck. The tumor can involve the cranial nerves by local compression, direct infiltration or by paraneoplastic process. Cranial nerve involvement depends on the anatomical course of the cranial nerve and the site of the tumor. Patients may present with single or multiple cranial n...
متن کاملProgressive multiple cranial nerve palsies as the presenting symptom of meningeal carcinomatosis from occult colon adenocarcinoma.
We herein describe a rare case of meningeal carcinomatosis in a 77-year-old woman who had bilateral deafness as the initial symptom of a previously undetected colon cancer malignancy. Meningeal carcinomatosis should be considered in the differential diagnosis in cases of abrupt-onset sensorineural deafness. Both MRI scans and cerebrospinal fluid evaluation are necessary diagnostic tools, and sh...
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BACKGROUND As an extremely rare subtype of sarcoidosis that develops exclusively in the nervous system, isolated neurosarcoidosis is difficult to diagnose. In addition, its exact clinical features are not known. CASE DESCRIPTION A 61-year-old man presented with right ear hearing loss, diplopia, and fever. Computed tomography (CT) and magnetic resonance imaging revealed mass lesions in the rig...
متن کاملGranulomatosis with polyangitis presenting with multiple cranial nerve palsies
Case presentation We report the case of localised granulomatosis with polyangitis in a 27 year old Caucasian gentleman who presented with multiple cranial neuropathies. He reported diplopia, hearing loss, dysphagia and dysarthria due to involvement of VI, XIII, IX, X and XII cranial nerves. A cerebral MRI demonstrated pachymeningitis along with mastoid changes and additional diagnostic workup s...
متن کاملRecurrent multiple cranial nerve palsies.
The material for this paper comprises four case reports, which must necessarily be presented in some detail, having regard to the points in which they resemble and differ from one another. The resemblance between these cases is close enough to suggest that they constitute a recognizable clinical syndrome. As to their aetiology, the data permit no definite conclusion but suggest the possibility ...
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ژورنال
عنوان ژورنال: Cancer
سال: 1982
ISSN: 0008-543X,1097-0142
DOI: 10.1002/1097-0142(19820415)49:8<1710::aid-cncr2820490829>3.0.co;2-h